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dc.contributor.authorCastellote Álvaro, María Isabel 
dc.contributor.authorVaquero López, Juan J.
dc.contributor.authorÁlvarez-Builla Gómez, Julio 
dc.date.accessioned2009-04-29T12:10:41Z
dc.date.available2009-04-29T12:10:41Z
dc.date.issued2004
dc.identifier.bibliographicCitationTetrahedron Letters, 2004, v. 45, n. 4, p. 769-772en
dc.identifier.issn0040-4039
dc.identifier.urihttp://hdl.handle.net/10017/2680
dc.description.abstractThe first intermolecular C–N bond-forming reactions between substituted 2-bromopyrroles and primary and cyclic secondary amines were performed using Pd2(dba)3 as catalyst with BINAP as the ligand. The aminations proceeded in the presence of NaOtBu at 80–100 °C in 31–93% yields.en
dc.description.sponsorshipFinancial support from the Comisión Interministerial de Ciencia y Tecnologı́a (CICYT, project BQU2001-1508) is gratefully acknowledged.en
dc.format.mimetypeapplication/pdfen
dc.language.isoengen
dc.publisherElsevieren
dc.rights(c) Elsevier, 2003en
dc.subjectPalladiumen
dc.subjectCatalyseden
dc.subjectAminationen
dc.subjectFunctionaliseden
dc.subject2-Halopyrrolesen
dc.subjectPyrrolodiazinesen
dc.subjectDerivativesen
dc.subjectChemistryen
dc.subjectChemistry, Organicen
dc.titlePalladium-catalysed amination of 2-acyl-1-alkyl-5-bromopyrrolesen
dc.typeinfo:eu-repo/semantics/articleen
dc.subject.ecienciaBioquímicaes_ES
dc.subject.ecienciaBiochemistryen
dc.subject.ecienciaScienceen
dc.subject.ecienciaCienciaes_ES
dc.contributor.affiliationUniversidad de Alcalá. Departamento de Química Orgánica
dc.relation.publisherversionhttp://dx.doi.org/10.1016/j.tetlet.2003.11.029
dc.type.versioninfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.1016/j.tetlet.2003.11.029
dc.relation.projectIDBQU2001-1508 (Comisión Interministerial de Ciencia y Tecnología-CICYT)
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessen


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